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Journal of Inherited Metabolic Disease|August 16, 2019
Fetal bovine serum impacts the observed N-glycosylation defects in TMEM165 KO HEK cellsDorothée Vicogne, Marine Houdou, Anne Garat, et al.Journal of Inherited Metabolic Disease|January 1, 1988
Clinical consequences of hyperlipidaemiaG R ThompsonJournal of Inherited Metabolic Disease|January 1, 1988
Biochemical, clinical, genetic and metabolic studies of hyperapo-beta-lipoproteinaemiaP O KwiterovichJournal of Inherited Metabolic Disease|March 4, 2021
Defective lysosomal storage in Fabry disease modifies mitochondrial structure, metabolism and turnover in renal epithelial cellsAnke Schumann, Kristin Schaller, Véronique Belche, et al.Journal of Inherited Metabolic Disease|October 7, 2019
Research priorities for liver glycogen storage disease: An international priority setting partnership with the James Lind AllianceFabian Peeks, Willemijn F Boonstra, Lut de Baere, et al.Journal of Inherited Metabolic Disease|May 11, 2011
Mitochondrial diabetes is associated with insulin resistance in subcutaneous adipose tissue but not with increased liver fat contentMarkus M Lindroos, Ronald Borra, Nina Mononen, et al.Journal of Inherited Metabolic Disease|June 1, 2011
Four-year follow-up of chronic neuronopathic Gaucher disease in Europeans using a modified severity scoring toolElin Haf Davies, Eugen Mengel, Anna Tylki-Szymanska, et al.Journal of Inherited Metabolic Disease|April 15, 2011
Dietary dilemmas in the management of glycogen storage disease type IKaustuv BhattacharyaJournal of Inherited Metabolic Disease|May 5, 2011
Interrupting the mechanisms of brain injury in a model of maple syrup urine disease encephalopathyWilliam J Zinnanti, Jelena LazovicPageof 429